Genomics & Informatics

Survey of the Applications of NGS to Whole-Genome Sequencing and Expression Profiling: Jong-Sung Lim, Beom-Soon Choi, Jeong-Soo Lee, Chanseok Shin, Tae-Jin Yang, Jae-Sung Rhee, Jae-Seong Lee, Ik-Young Choi; Genomics Inform. 2012;10(1):1-8. Published online March 31, 2012; DOI: https://doi.org/10.5808/GI.2012.10.1.1
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Estimation of the Genetic Substitution Rate of Hanwoo and Holstein Cattle Using Whole Genome Sequencing Data: Young-Sup Lee, Donghyun Shin; Genomics Inform. 2018;16(1):14-20. Published online March 30, 2018; DOI: https://doi.org/10.5808/GI.2018.16.1.14
Cited By 4; Full text PubReader ePub PDF Supplementary Material

Ultra-rare Disease and Genomics-Driven Precision Medicine: Sangmoon Lee, Murim Choi; Genomics Inform. 2016;14(2):42-45. Published online June 30, 2016; DOI: https://doi.org/10.5808/GI.2016.14.2.42
Cited By 9; Full text PubReader ePub PDF

A Simple Java Sequence Alignment Editing Tool for Resolving Complex Repeat Regions.: Seong Il Ham, Kyung Eun Lee, Hyun Seok Park; Genomics Inform. 2009;7(1):46-48.; DOI: https://doi.org/10.5808/gi.2009.7.1.046; PDF

Analysis of genome variants in dwarf soybean lines obtained in F6 derived from cross of normal parents (cultivated and wild soybean): Neha Samir Roy, Yong-Wook Ban, Hana Yoo, Rahul Vasudeo Ramekar, Eun Ju Cheong, Nam-Il Park, Jong Kuk Na, Kyong-Cheul Park, Ik-Young Choi; Genomics Inform. 2021;19(2):e19. Published online June 30, 2021; DOI: https://doi.org/10.5808/gi.21024
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Chromosome-specific polymorphic SSR markers in tropical eucalypt species using low coverage whole genome sequences: systematic characterization and validation: Maheswari Patturaj, Aiswarya Munusamy, Nithishkumar Kannan, Ulaganathan Kandasamy, Yasodha Ramasamy; Genomics Inform. 2021;19(3):e33. Published online September 30, 2021; DOI: https://doi.org/10.5808/gi.21031
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Whole genome sequence analyses of thermotolerant Bacillus sp. isolates from food: Phornphan Sornchuer, Kritsakorn Saninjuk, Pholawat Tingpej; Genomics Inform. 2023;21(3):e35. Published online September 27, 2023; DOI: https://doi.org/10.5808/gi.23030
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Analysis of unmapped regions associated with long deletions in Korean whole genome sequences based on short read data: Yuna Lee, Kiejung Park, Insong Koh; Genomics Inform. 2019;17(4):e40. Published online December 20, 2019; DOI: https://doi.org/10.5808/GI.2019.17.4.e40
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Metagenomic analysis of viral genes integrated in whole genome sequencing data of Thai patients with Brugada syndrome: Suwalak Chitcharoen, Chureerat Phokaew, John Mauleekoonphairoj, Apichai Khongphatthanayothin, Boosamas Sutjaporn, Pharawee Wandee, Yong Poovorawan, Koonlawee Nademanee, Sunchai Payungporn; Genomics Inform. 2022;20(4):e44. Published online December 30, 2022; DOI: https://doi.org/10.5808/gi.22047
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Functional annotation of de novo variants from healthy individuals: Jean Lee, Sung Eun Hong; Genomics Inform. 2019;17(4):e46. Published online December 23, 2019; DOI: https://doi.org/10.5808/GI.2019.17.4.e46; Full text PubReader ePub PDF

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